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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AMILORIDE\FUROSEMIDE Cause Product use issue? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use issue have been filed in association with AMILORIDE\FUROSEMIDE. This represents 7.9% of all adverse event reports for AMILORIDE\FUROSEMIDE.

6
Reports of Product use issue with AMILORIDE\FUROSEMIDE
7.9%
of all AMILORIDE\FUROSEMIDE reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product use issue From AMILORIDE\FUROSEMIDE?

Of the 6 reports, 6 (100.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMILORIDE\FUROSEMIDE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does AMILORIDE\FUROSEMIDE Cause?

Hyperkalaemia (22) Hyponatraemia (19) Muscular weakness (15) Orthostatic hypotension (12) Diabetic ketoacidosis (11) Renal impairment (9) Wernicke's encephalopathy (7) Blood creatinine increased (6) Blood sodium increased (6) Blood urea increased (6)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

AMILORIDE\FUROSEMIDE Full Profile All Product use issue Reports All Drugs Causing Product use issue AMILORIDE\FUROSEMIDE Demographics